Patents
Literature
Patsnap Eureka AI that helps you search prior art, draft patents, and assess FTO risks, powered by patent and scientific literature data.

11 results about "P2x7 receptor" patented technology

P2X7 receptors are extracellular ATP-gated ion channels that play broad physiological and pathological roles in animals (Sluyter, 2017). Activation of P2X7 receptors lead to the opening of membrane channels permeable for small cations like Na + and Ca 2+ as well as fluorescent dyes such as YO-PRO-1 (Alves et al., 2014).

P2x7 receptor antagonists

Described herein are compounds of formula (I), where the substituents are disclosed herein, and exhibit antagonistic and / or inhibitory activity against the P2X7 receptor. These compounds, and their pharmaceutically acceptable salts, hydrates, solvates, and compositions thereof, are suitable for use in the prevention and treatment of diseases and conditions modulated by inhibition of the P2X7 receptor.
Owner:BREYE THERAPEUTICS APS

Treatment of hyperinflammatory syndrome

To provide a method for treatment of patients suffering from a hyperinflammatory syndrome without hampering the inflammatory response of the patients or at least to a much lesser extent.SOLUTION: Provided is an antagonist of a mammalian P2X7 receptor (P2X7R) for use in the treatment of a hyperinflammatory syndrome in a mammalian patient, by primary lymph node targeted administration of the P2X7R antagonist in the patient to a concentration of the antagonist of the mammalian P2X7R in the targeted lymph nodes that is above the maximal tolerable plasma level of the antagonist in the mammal.SELECTED DRAWING: None
Owner:REMICINE IP BV

Nanoclusters Functionalized with Adenosine Triphosphate or an Analogue and Their Use

Compositions, methods, and kits are provided for treating infections and cancer with metallic nanoclusters. In particular, metallic nanoclusters having a size of less than 10 nm that are conjugated to adenosine triphosphate (ATP) or an analogue thereof can be used to eradicate a cell in a growth arrest phase such as infectious bacterial or fungal cells. Such nanoclusters can also induce endoplasmic reticulum stress and inhibit growth of cancerous cells. Additionally, such metallic nanoclusters can be used to inhibit a purinergic P2X7 receptor and FtsH protease.
Owner:THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIV

Heterocyclic derivatives as P2X7 receptor antagonists

The present invention relates to novel 1,4-substituted piperidine compounds of formula (I) having P2X7 receptor (P2X7) antagonistic properties, pharmaceutical compositions containing these compounds, chemical processes for preparing these compounds, and their use in the treatment or prevention of diseases associated with P2X7 receptor activity in animals, particularly humans.
Owner:ブルイエ·セラピューティクス·アー·ペー·エス

Heterocyclic derivatives as P2X7 receptor antagonists

The present invention relates to novel 1,4-substituted piperidine compounds of formula (I) having P2X7 receptor (P2X7) antagonistic properties, pharmaceutical compositions comprising these compounds, chemical processes for preparing these compounds and their use in the treatment or prophylaxis of diseases associated with P2X7 receptor activity in animals, in particular humans.
Owner:BREYE THERAPEUTICS APS

N-arylbenzamide derivatives as P2X7 receptor antagonists

The present invention relates to novel N-arylbenzamide derivatives of formula (I) or isotopic forms, stereoisomers or pharmaceutically acceptable salts thereof as P2X7 receptor antagonists. The invention also relates to pharmaceutical compositions comprising such compounds, chemical processes for preparing such compounds and the use of such compounds in the treatment or prevention of diseases or conditions associated with P2X7 receptor activity.
Owner:SUVEN LIFE SCI LTD